Cancer Immunotherapy: Beyond Checkpoint Blockade

被引:99
|
作者
Dougan, Michael [1 ,2 ,3 ]
Dranoff, Glenn [4 ]
Dougan, Stephanie K. [3 ,5 ]
机构
[1] Massachusetts Gen Hosp, Div Gastroenterol, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[3] Harvard Univ, Harvard Med Sch, Boston, MA 02115 USA
[4] Novartis Inst Biomed Res, Cambridge, MA 02139 USA
[5] Dana Farber Canc Inst, Dept Canc Immunol & Virol, Boston, MA 02215 USA
关键词
immunotherapy; cancer; antitumor immunity; checkpoint blockade; toxicity; oncogenic inflammation; combination therapy; CHIMERIC ANTIGEN RECEPTOR; ENDOTHELIAL GROWTH-FACTOR; T-CELL PROLIFERATION; TERM-FOLLOW-UP; REGULATORY T; ANTITUMOR IMMUNITY; TGF-BETA; CYTOKINE PRODUCTION; DENDRITIC CELLS; COMBINATION IMMUNOTHERAPY;
D O I
10.1146/annurev-cancerbio-030518-055552
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Blocking antibodies to the immune checkpoint receptors or their ligands have revolutionized the treatment of diverse malignancies. Many tumors are recognized by adaptive immunity, but these adaptive responses can be inhibited by immunosuppressive mechanisms within the tumor, often through pathways outside of the currently targeted checkpoints. For this reason, only a minority of cancer patients achieve durable responses to current immunotherapies. Multiple novel approaches strive to expand immunotherapy's reach. These may include targeting alternative immune checkpoints. However, many investigational strategies look beyond checkpoint blockade. These include cellular therapies to bypass endogenous immunity and efforts to stimulate new adaptive antitumor responses using vaccines, adjuvants, and combinations with cytotoxic therapy, as well as strategies to inhibit innate immune suppression and modulate metabolism within the tumor microenvironment. The challenge for immunotherapy going forward will be to select rational strategies for overcoming barriers to effective antitumor responses from the myriad possible targets.
引用
收藏
页码:55 / 75
页数:21
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